Diels–Alder reaction of quinones generated in situ by electrochemical oxidation in lithium perchlorate–nitromethane

1994 ◽  
Vol 0 (21) ◽  
pp. 2485-2486 ◽  
Author(s):  
Kazuhiro Chiba ◽  
Masahiro Tada
Keyword(s):  
Electrochemical Oxidation ◽  
Lithium Perchlorate ◽  
Alder Reaction ◽  
Diels Alder ◽  
Diels Alder Reaction

Lithium perchlorate catalysis of the hetero Diels-Alder reaction: a specific lithium cation effect.

Tetrahedron ◽  
1991 ◽  
Vol 47 (39) ◽  
pp. 8399-8406 ◽  
Author(s):  
G. Desimoni ◽  
G. Faita ◽  
P.P. Righetti ◽  
G. Tacconi
Keyword(s):  
Lithium Perchlorate ◽  
Alder Reaction ◽  
Diels Alder ◽  
Lithium Cation ◽  
Cation Effect ◽  
Diels Alder Reaction

Organocatalytic enantioselective Diels–Alder reaction between hydroxymaleimides and in situ generated nitrosoalkenes for direct preparation of chiral hemiketals with 1,2-oxazine skeleton

2021 ◽  
Author(s):  
Min Xiang ◽  
Chen-Yi Li ◽  
Jian Zhang ◽  
Ying Zou ◽  
Wen-Sheng Li ◽  
...  
Keyword(s):  
Alder Reaction ◽  
Diels Alder ◽  
Diels Alder Reaction ◽  
Direct Preparation

Organocatalytic Enantioselective IEDDA reaction between hydroxymaleimides and in situ generated nitrosoalkenes has been disclosed, a series of chiral hemiketals containing 5,6-dihydro-4H-l,2-oxazines and succinimide frameworks have been prepared.

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